Dichloromethane → HCID 67119774, compound

Participants

Reaction Conditions

Reaction Steps

N-(1-(4-morpholinophenyl)ethyl)-4-benzoylmethyl-4-piperidinol (III-27) is firstly prepared according to the method of synthesis and post-treatment in Example 27. 1.63 g (4.0 mmol) of N-(1-(4-morpholino phenyl)ethyl)-4-benzoylmethyl-4-piperidinol is dissolved into 20 ml of anhydrous dichloromethane and cooled with dry ice-acetone with temperature controlled at below <−70° C. The reaction solution is added dropwise a dichloromethane solution (8 mol, 25 ml) of DAST protecting of nitrogen gas. After completion of addition, the temperature is maintained at −75° C. and reacting for 1 hour, and the temperature is raised slowly and maintained at −10° C. and reacting for 2 hours. Then operating according to the post-treatment method in General Method six obtains 0.81 g of a white crystal, with yield of 40.5%.

Provenance & Evidence